A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746996



Internal ID20523012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2876494..2876640hg38UCSC Ensembl
chr18:2876492..2876638hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259233
Samples
Known GenesEMILIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746996
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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